Dofetilide
- Product NDC
- 16714-841
- 11-digit product format
- 167140841
- Labeler code
- 16714
- Product ID
- 16714-841_c8bb2a18-e47e-4e85-a052-85b06cd221e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dofetilide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA207058
- Marketing category
- ANDA
- Marketing start
- 2018-06-18
- Marketing end
- 0000-00-00
- Substance
- DOFETILIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-841-01 | 16714084101 | 60 CAPSULE in 1 BOTTLE, PLASTIC (16714-841-01) | 60 capsule | 2018-06-18 | 0000-00-00 | No | No | Current |